SHMT1 anticorps

N° du produit ABIN2854425

Cet anticorps anti-SHMT1 est un anticorps Lapin Polyclonal détectant SHMT1 dans WB. Adapté pour Humain.

Aperçu rapide pour SHMT1 anticorps (ABIN2854425)

Antigène: SHMT1 (serine Hydroxymethyltransferase 1 (Soluble) (SHMT1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SHMT1 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-SHMT1 anticorps

Réactivité croisée: Humain

Attributs du produit: Rabbit Polyclonal antibody to SHMT1 (serine hydroxymethyltransferase 1 (soluble))
SHMT1 antibody

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein encompassing a sequence within the center region of human SHMT1. The exact sequence is proprietary.

Isotype: IgG

Information d'application

Indications d'application: WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Commentaires:

Positive Control: U87-MG

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: 1XPBS ( pH 7), 1 % BSA, 20 % Glycerol, 0.01 % Thimerosal

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Détails sur SHMT1

Antigène: SHMT1 (serine Hydroxymethyltransferase 1 (Soluble) (SHMT1))

Autre désignation: serine hydroxymethyltransferase 1

Sujet: This gene encodes the cellular form of serine hydroxymethyltransferase, a pyridoxal phosphate-containing enzyme that catalyzes the reversible conversion of serine and tetrahydrofolate to glycine and 5,10-methylene tetrahydrofolate. This reaction provides one carbon units for synthesis of methionine, thymidylate, and purines in the cytoplasm. This gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternative splicing of this gene results in 2 transcript variants encoding 2 different isoforms. Additional transcript variants have been described, but their biological validity has not been determined.

Cellular Localization: Cytoplasm

Poids moléculaire: 53 kDa

ID gène: 6470

UniProt: P34896